CSF inflammatory markers and neurocognitive function after addition of maraviroc to monotherapy darunavir/ritonavir in stable HIV patients: the CINAMMON study.
Tristan J BarberA ImazM BoffitoJ NiubóA PozniakR FortunyJ AlonsoN DaviesS MandaliaD PodzamczerB GazzardPublished in: Journal of neurovirology (2017)
CINAMMON is a phase IV, open-label, single-arm, pilot study assessing maraviroc (MVC) in the central nervous system (CNS) when added to darunavir/ritonavir monotherapy (DRV/r) in virologically suppressed HIV-infected subjects. CCR5 tropic participants on DRV/r were recruited. Participants remained on DRV/r for 12 week (w) (control phase). MVC 150 mg qd was added w12-w36 (intervention phase). Lumbar puncture (LP) and neurocognitive function (Cogstate) examinations scheduled at baseline, w12 and w36; MRI before w12, again at w36. Primary endpoint was CSF inflammatory marker changes during intervention phase. Secondary endpoints included changes in NC function and MRI parameters. CSF/plasma DRV/r concentrations measured at w12 and w36, MVC at w36. Nineteen patients recruited, 15 completed (17M, 2F). Dropouts: headache (2), knee problem (could not attend, 1), personal reasons (1). Mean age (range) 45.4 years (27.2-65.1), 13/19 white, 10/19 MSM. No changes in selected CSF markers were seen w12-w36. Overall NC function did not improve w12-w36: total age adjusted z score improved by 0.27 (weighted paired t test; p = 0.11); for executive function only, age adjusted z score improved by 0.54 (p = 0.03). MRI brain parameters unchanged. DRV plasma:CSF concentration ratio unchanged between w12 (132) and w36 (112; p = 0.577, Wilcoxon signed-rank). MVC plasma:CSF concentration ratio was 35 at w36. No changes in neuroinflammatory markers seen. In this small study, addition of 24w MVC 150 mg qd to stable DRV/r monotherapy showed possible improvement in executive function with no global NC effect. Learning effect cannot be excluded. This effect should be further evaluated.
Keyphrases
- hiv infected
- open label
- antiretroviral therapy
- magnetic resonance imaging
- contrast enhanced
- end stage renal disease
- hiv infected patients
- ejection fraction
- randomized controlled trial
- newly diagnosed
- combination therapy
- cerebrospinal fluid
- clinical trial
- prognostic factors
- magnetic resonance
- hepatitis c virus
- bipolar disorder
- oxidative stress
- hiv positive
- blood brain barrier
- immune response
- patient reported outcomes
- minimally invasive
- multiple sclerosis
- dendritic cells
- functional connectivity
- resting state
- white matter
- south africa
- radiation therapy
- regulatory t cells
- phase ii study